EP0981334A1 - Comprimes a avaler contenant du paracetamol - Google Patents

Comprimes a avaler contenant du paracetamol

Info

Publication number
EP0981334A1
EP0981334A1 EP98913664A EP98913664A EP0981334A1 EP 0981334 A1 EP0981334 A1 EP 0981334A1 EP 98913664 A EP98913664 A EP 98913664A EP 98913664 A EP98913664 A EP 98913664A EP 0981334 A1 EP0981334 A1 EP 0981334A1
Authority
EP
European Patent Office
Prior art keywords
paracetamol
sodium bicarbonate
tablet
tablets
starch
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP98913664A
Other languages
German (de)
English (en)
Other versions
EP0981334B1 (fr
Inventor
Timothy James Grattan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SmithKline Beecham Ltd
Original Assignee
SmithKline Beecham Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SmithKline Beecham Ltd filed Critical SmithKline Beecham Ltd
Priority to SI9830474T priority Critical patent/SI0981334T1/xx
Publication of EP0981334A1 publication Critical patent/EP0981334A1/fr
Application granted granted Critical
Publication of EP0981334B1 publication Critical patent/EP0981334B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2009—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/485—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect

Definitions

  • the present invention relates to pharmaceutical compositions containing N- acetyl-p-aminophenol, known by the generic names paracetamol, acetaminophen and APAP (hereinafter referred to as paracetamol).
  • paracetamol N- acetyl-p-aminophenol
  • the invention relates to a fast acting paracetamol formulation in the form of a swallow tablet or capsule which has a greatly improved rate of absorption following ingestion by the patient.
  • Paracetamol is an analgesic and antipyretic agent which is widely used in prescription and non-prescription medicines, often in combination with other biologically active compounds.
  • a solid form such as a tablet or capsule
  • the rate of absorption and hence the onset of pharmacological activity has been found to vary from patient to patient and can sometimes be very slow.
  • Many attempts have been made to improve the rate of onset of activity, for example by speeding up the disintegration of tablets by making effervescent formulations.
  • United Kingdom patent publication GB 2 103 087 (Bristol-Myers) describes an analgesic composition containing paracetamol that has an increased rate of absorption.
  • GB 2 103 087 refers to a publication (J. Wojcicki et al, Zbl. Pharm. , 118, (1979), Vol 2-3) describing investigations into the pharmacokinetics of paracetamol in which a single oral dose of 1000 mg of paracetamol was administered with 4000 mg of antacid in the form of calcium carbonate. According to the reference in GB 2 103 087, the combination was found to decrease the rate of absorption of paracetamol, when compared with the rate of absorption from paracetamol (1000 mg ) alone.
  • an improved rate of absorption is achieved by co-administering a therapeutic dose comprising from about 150 mg to about 2000 mg of paracetamol with from about 60 mg to about 1200 mg of an antacid.
  • a therapeutic dose comprising from about 150 mg to about 2000 mg of paracetamol with from about 60 mg to about 1200 mg of an antacid.
  • the publication states that any antacid or combinations thereof commonly used to neutralise stomach acids may be used.
  • GB 2 103 087 identifies antacids of special interest to be calcium carbonate, magnesium carbonate, a combination of calcium carbonate and magnesium carbonate, sodium bicarbonate and magnesium hydroxide.
  • GB 2 103 087 exemplifies compositions comprising combinations of paracetamol with calcium carbonate, with a mixture of calcium carbonate and magnesium carbonate and with sodium bicarbonate.
  • the examples in GB 2 103 087 include two tablet formulations containing paracetamol and sodium bicarbonate; one such formulation comprises 325 mg of paracetamol and 225 mg of sodium bicarbonate wherein the weight ratio of sodium bicarbonate to paracetamol is 0.69 to 1, and the second formulation comprises 500 mg of paracetamol and 225 mg of sodium bicarbonate wherein the weight ratio of sodium bicarbonate to paracetamol is 0.4 to 1.
  • the various formulations exemplified in GB 2 103 087 were administered to healthy volunteers it was found that, for all the formulations tested, the actual increase in rate of absorption, was between 7 and 31 % compared to conventional paracetamol tablets.
  • the rate of absorption following oral admimstration of such a solid dosage form comprising paracetamol and sodium bicarbonate also shows an improvement over that obtained following oral admimstration of an aqueous solution of a commercially available soluble product containing paracetamol and sodium bicarbonate.
  • an increase in the rate of abso ⁇ tion may be demonstrated as an increased in C max , where C rozx is the maximum concentration of paracetamol in the serum, or by measuring the area under the concentration vs time curve in the first 20 minutes after dosing (AUC 0-2 o) when compared with other paracetamol compositions.
  • a swallow tablet or capsule formulation comprising from 300mg to 600mg of paracetamol and from 300mg to 1200mg of sodium bicarbonate wherein the weight ratio of sodium bicarbonate to paracetamol is at least 0.74 to 1.
  • a swallow tablet is a tablet which is intended to be swallowed whole and not one which is intended for dissolution or suspension in water prior to administration, for example a tablet containing a substantial amount of an effervescent couple.
  • the tablet or capsule formulation of the invention preferably contains either 325 mg or 500 mg of paracetamol.
  • the amount of sodium bicarbonate present in the formulation is favourably at least 370 mg, eg at least 400 mg or 500 mg and suitably is no greater than 1000 mg, preferably no greater than 800 mg and more preferably no greater than 700 mg.
  • the weight ratio of sodium bicarbonate to paracetamol is favourably at least 0.8 to 1, preferably at least 1 to 1, and more preferably at least 1.25 to 1.
  • Formulations of the invention will generally contain at least one pharmaceutically acceptable excipient conventionally used in the art of tablet and/or capsule formulation.
  • Suitable excipients which may be inco ⁇ orated include lubricants, for example magnesium stearate and stearic acid; disintegrants, for example cellulose derivatives; starches; binders, for example modified starches and cellulose derivatives; glidants, for example colloidol silicas; compression aids, for example cellulose derivatives; as well as preservatives, suspending agents, wetting agents, flavouring agents, bulking agents, adhesives, colouring agents, sweetening agents appropriate to their form.
  • formulations of the invention may also contain other pharmaceutically active agents, for example other analgesics, anti- inflammatory analgesic agents, decongestants, antihistamines, antitussive agents, etc..
  • Formulations may also contain a pharmaceutically acceptable analgesic adjuvant, for example caffeine.
  • the invention also provides a process for the preparation of the tablet or capsule formulation of the invention, which process comprises the admixture of paracetamol and sodium bicarbonate together with any pharmaceutically acceptable excipients, additional pharmaceutically acceptable active agents or adjuvants.
  • the paracetamol and sodium bicarbonate may be mixed together with one or more binders and granulated using water.
  • the resulting granule may then be dried, sieved and mixed with additional excipients such as a lubricant and disintegrant before being compressed into tablets.
  • additional excipients such as a lubricant and disintegrant
  • the sodium bicarbonate may be omitted from the granulation step and subsequently added with the other excipients.
  • tablets may be prepared using direct compression grades of paracetamol including commercially available forms which obviates the need for a granulation step. Tablets may also be prepared by other processes known in the art such as by shaping of an extruded mixture.
  • the paracetamol and sodium bicarbonate may be mixed and granulated as for tablet production and filled into suitably sized capsule shells to the desired fill weight.
  • the formulations according to the invention have an increased C ⁇ , where C max is the maximum concentration of paracetamol in the serum, when compared with other paracetamol compositions. Comparative experiments have demonstrated an increased C ⁇ with respect to that obtained not only from swallow tablets containing only paracetamol or paracetamol plus calcium carbonate but also from proprietary soluble paracetamol formulations. Furthermore the formulations according to the invention have an increased (AUC 0 . 20 ), indicating an increased rate of abso ⁇ tion of paracetamol, when compared to conventional paracetamol swallow tablets. .
  • the plasma profile for the paracetamol formulations in accordance with the present invention is comparable to that expected to be achieved with a dose of paracetamol administered intravenously.
  • Intravenous dosing of drugs is generally recommended in order to achieve a rapid maximum therapeutic effect which is not obtainable via oral dosing.
  • intravenous dosing can be both painful and inconvenient.
  • the present invention accordingly offers considerable practical benefit.
  • the addition of sodium bicarbonate in the weight ratio of the present invention has the potential added advantage that it may reduce the potential for patients to suffer toxic effects of paracetamol overdose, which can have fatal consequences or, at the very least, lead to irreversible liver damage.
  • An intake of about 40 paracetamol tablets containing 500mg paracetamol usually causes serious liver damage and sometimes proves fatal.
  • the emetic dose of sodium bicarbonate is such that for most patients it would be achieved after swallowing tablets of the present invention well before the intake of paracetamol reaches a level that would prove fatal.
  • formulations of the present invention are clearly of benefit.
  • a granule suitable for compression into tablets was prepared from the following ingredients
  • Tablets were prepared from the following ingredients:
  • Each tablet contained paracetamol 500mg and sodium bicarbonate 630mg, with a ratio of sodium bicarbonate: paracetamol of 1.26 : 1
  • Example 3
  • Tablets (target weight 1023.82mg) were prepared by a similar method to than described in examples 1 and 2, but using different levels of ingredients such that the final formula was as follows:
  • Each tablet contained paracetamol 500mg and sodium bicarbonate 400mg, with a ratio of sodium bicarbonate: paracetamol of 0.8 : 1
  • Tablets (target weight 993.82mg) are prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients such that the final formula is as follows:
  • Each tablet contains paracetamol 500mg and sodium bicarbonate 370mg, with a ratio of sodium bicarbonate: paracetamol of 0.74 : 1
  • Example 5
  • Tablets (target weight 1430.7mg) are prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients such that the final formula is as follows:
  • Each tablet contains paracetamol 500mg and sodium bicarbonate 800 mg, with a ratio of sodium bicarbonate: paracetamol of 1.6 : 1
  • Tablets (target weight 923.82mg) are prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients such that the final formula is as follows:
  • Each tablet contains paracetamol 400mg and sodium bicarbonate 400mg, with a ratio of sodium bicarbonate: paracetamol of 1 : 1
  • Example 7
  • Tablets (target weight 1223.82mg) are prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients such that the final formula is as follows:
  • Each tablet contains paracetamol 600mg and sodium bicarbonate 500mg, with a ratio of sodium bicarbonate: paracetamol of 0.83 : 1
  • Tablets (target weight 819.46mg) are prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients such that the final formula is as follows:
  • Each tablet contains paracetamol 325mg and sodium bicarbonate 409.5mg, with a ratio of sodium bicarbonate to paracetamol of 1.26 : 1
  • Example 9
  • Tablets (target weight 1291.56mg) are prepared by blending ingredients 1 to 7 together and compressing using a suitable tablet press:
  • Each tablet contains paracetamol 500mg and sodium bicarbonate 630mg, with a ratio of sodium bicarbonate to paracetamol of 1.26 : 1
  • Capsules are prepared as follows:
  • Each capsule contains paracetamol 325mg and sodium bicarbonate 409.5mg, with a ratio of sodium bicarbonate to paracetamol of 1.26 : 1 Comparative Example A
  • Tablets (target weight 988.23mg) were prepared by a similar method to that described in examples 1 and 2, but using different levels of ingredients and substituting calcium carbonate for sodium bicarbonate, such that the final formula was as follows:
  • Each tablet contained paracetamol 500mg and calcium carbonate 375 mg, with ratio of calcium carbonate to paracetamol of 0.75 : 1
  • test formula E the 2 tablets were dissolved in the lOOmls of water prior to swallowing.
  • Blood samples were taken at 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 75, 90, 120, 180, 240, 360, 480, and 720 minutes post dose.
  • Serum paracetamol levels were determined by HPLC and paracetamol serum levels vs time profiles were plotted for each volunteer. There were no significant differences in the area under the serum level vs time curve (AUC 0 ⁇ ,) for any of the formulae.
  • the Cmax for formula A was statistically significantly higher than that seen for formula C (p ⁇ 0 .0002), D (p ⁇ 0.002) and E (PO.02). There was no statistically significant difference between the Cmax for formula A and B.
  • the Cmax for formula B was significantly higher than that seen for formula C (p ⁇ 0.01) and formula D (p ⁇ 0.02)
  • test formula A 245 mg.min/L test formula B 177 mg.min/L test formula C 76.0 mg . min/L test formula D 69.7 mg.min/L test formula E 199 mg.min/L
  • the (AUC 0 . 20 ) for formulation A was 3.5 times greater than for formulation D and the (AUC 0 . 20 ) for formulation B was 2.5 times greater than for formulation D, both of these differences were statistically significant, indicating that the rate of paracetamol abso ⁇ tion from the invention was increased by a factor of up to 250% compared to conventional paracetamol swallow tablets.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Inorganic Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Rheumatology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Detergent Compositions (AREA)

Abstract

L'invention concerne une formulation pour gélule ou comprimé, à administrer par voie orale, contenant du paracétamol, du bicarbonate de sodium et au moins un excipient pharmaceutiquement acceptable.
EP98913664A 1997-03-05 1998-02-27 Comprimes a avaler contenant du paracetamol Expired - Lifetime EP0981334B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SI9830474T SI0981334T1 (en) 1997-03-05 1998-02-27 Swallow tablet comprising paracetamol

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9704524 1997-03-05
GBGB9704524.9A GB9704524D0 (en) 1997-03-05 1997-03-05 Composition
PCT/EP1998/001284 WO1998038983A2 (fr) 1997-03-05 1998-02-27 Comprimes a avaler contenant du paracetamol

Publications (2)

Publication Number Publication Date
EP0981334A1 true EP0981334A1 (fr) 2000-03-01
EP0981334B1 EP0981334B1 (fr) 2003-05-21

Family

ID=10808717

Family Applications (1)

Application Number Title Priority Date Filing Date
EP98913664A Expired - Lifetime EP0981334B1 (fr) 1997-03-05 1998-02-27 Comprimes a avaler contenant du paracetamol

Country Status (36)

Country Link
US (1) US6316025B1 (fr)
EP (1) EP0981334B1 (fr)
JP (1) JP2001513801A (fr)
KR (1) KR100465895B1 (fr)
CN (1) CN100389751C (fr)
AP (1) AP1084A (fr)
AR (1) AR011919A1 (fr)
AT (1) ATE240720T1 (fr)
AU (1) AU721851B2 (fr)
BG (1) BG64348B1 (fr)
BR (1) BR9807992A (fr)
CA (1) CA2283408C (fr)
CO (1) CO4940406A1 (fr)
CY (1) CY2367B1 (fr)
CZ (1) CZ294078B6 (fr)
DE (1) DE69814850T2 (fr)
DK (1) DK0981334T3 (fr)
EA (1) EA001918B1 (fr)
ES (1) ES2199435T3 (fr)
GB (1) GB9704524D0 (fr)
HK (1) HK1027026A1 (fr)
HU (1) HU224983B1 (fr)
ID (1) ID22233A (fr)
IL (1) IL131552A (fr)
MY (1) MY119722A (fr)
NO (1) NO327456B1 (fr)
NZ (1) NZ337418A (fr)
PE (1) PE68899A1 (fr)
PL (1) PL190988B1 (fr)
PT (1) PT981334E (fr)
SK (1) SK282277B6 (fr)
TR (1) TR199902175T2 (fr)
TW (1) TW508242B (fr)
UA (1) UA59388C2 (fr)
WO (1) WO1998038983A2 (fr)
ZA (1) ZA981832B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6211246B1 (en) 1999-06-10 2001-04-03 Mcneil-Ppc, Inc. Rapidly absorbed liquid compositions
NZ508291A (en) * 1999-11-24 2002-09-27 Mcneil Ppc Inc Use of acetaminophen in a medicament for treating migraine symptoms
GB0006897D0 (en) * 2000-03-23 2000-05-10 Smithkline Beecham Plc Medicaments
GB0114069D0 (en) 2001-06-08 2001-08-01 Smithkline Beecham Plc Composition
GB0129117D0 (en) * 2001-12-05 2002-01-23 Glaxo Group Ltd Pharmaceutical composition
JP2006522790A (ja) * 2003-04-11 2006-10-05 ファイザー・インク エレトリプタンと重炭酸ナトリウムを含む医薬組み合わせ物
US8216610B2 (en) * 2004-05-28 2012-07-10 Imaginot Pty Ltd. Oral paracetamol formulations
CA2566331C (fr) * 2004-05-28 2011-03-15 Imaginot Pty Ltd. Systeme d'administration par voie orale
US20080287456A1 (en) 2004-05-28 2008-11-20 Imaginot Pty Ltd Oral Therapeutic Compound Delivery System
DE102004042139B4 (de) * 2004-08-31 2009-06-10 Aristocon Verwaltungs- Gmbh Perorale Darreichungsformen zur Erzielung eines Retardierungseffektes nach der Arzneimitteleinnahme mit einer Mahlzeit
CN101048155A (zh) * 2004-10-28 2007-10-03 诺瓦提斯公司 含有对乙酰氨基酚、咖啡因和任选的阿司匹林以及用于增强吸收的碱性剂的组合物
US9060950B2 (en) * 2005-06-13 2015-06-23 Paul H. Rosenberg, Proximate Concepts, LLC. Emetic embedded capsule
CA2612044C (fr) * 2005-06-13 2016-02-02 Paul Rosenberg Capsule contenant un emetique
KR100702069B1 (ko) * 2005-10-31 2007-03-30 (주)이엘티사이언스 파라세타몰 경구용 수용산제 복합조성물 및 그 제조방법
JP2009517346A (ja) 2005-11-28 2009-04-30 イメイジノット ピーティーワイ エルティーディー 治療用化合物の経口送達系
GB0607085D0 (en) * 2006-04-07 2006-05-17 Smithkline Beecham Corp Novel compositions
WO2008008120A1 (fr) * 2006-07-14 2008-01-17 Fmc Corporation Forme solide
US20080311162A1 (en) * 2007-05-16 2008-12-18 Olivia Darmuzey Solid form
EP2203165B1 (fr) 2007-08-07 2013-05-22 Stellenbosch University Paracetamol pour l'utilisation dans le traitement du glaucome
KR101687580B1 (ko) 2016-07-19 2016-12-20 주식회사 씨.월드 의자 등받이부와 프레임부 조립구조
CA3115122A1 (fr) 2018-11-19 2020-05-28 Jazz Pharmaceuticals Ireland Limited Formulations de medicament resistant a l'alcool

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1182049A (fr) 1981-07-13 1985-02-05 Francis J. Sterbenz Compose d'apap et d'antiacide
US4942039A (en) * 1989-05-09 1990-07-17 Miles Inc. Effervescent analgesic antacid composition having reduced sodium content
ES2060736T3 (es) * 1989-01-12 1994-12-01 Bayer Ag Composicion antiacida analgesica efervescente con un contenido en sodio reducido.
US5348745A (en) * 1989-05-09 1994-09-20 Miles Inc. Aqueous granulation solution and a method of tablet granulation
CA2021548A1 (fr) * 1989-09-01 1991-03-02 Ronald Nash Duvall Compose medicinal effervescent a teneur reduite en sodium pour le soulagement des symptomes du rhume et des allergies
DE19502789A1 (de) 1995-01-28 1996-08-01 Dirk Krischenowski Arzneimittel

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9838983A2 *

Also Published As

Publication number Publication date
JP2001513801A (ja) 2001-09-04
AU6828298A (en) 1998-09-22
CN100389751C (zh) 2008-05-28
PL335502A1 (en) 2000-04-25
SK119799A3 (en) 2000-02-14
CA2283408A1 (fr) 1998-09-11
AR011919A1 (es) 2000-09-13
DK0981334T3 (da) 2003-09-22
TR199902175T2 (xx) 1999-12-21
CN1253497A (zh) 2000-05-17
CZ294078B6 (cs) 2004-09-15
HUP0001501A3 (en) 2001-01-29
KR100465895B1 (ko) 2005-01-13
HUP0001501A2 (hu) 2000-09-28
US6316025B1 (en) 2001-11-13
CA2283408C (fr) 2007-01-02
PE68899A1 (es) 1999-09-26
DE69814850T2 (de) 2004-03-11
ES2199435T3 (es) 2004-02-16
UA59388C2 (uk) 2003-09-15
ID22233A (id) 1999-09-23
EA001918B1 (ru) 2001-10-22
WO1998038983A2 (fr) 1998-09-11
AP9901638A0 (en) 1999-09-30
CO4940406A1 (es) 2000-07-24
CY2367B1 (en) 2004-06-04
ATE240720T1 (de) 2003-06-15
IL131552A (en) 2004-08-31
BG103714A (en) 2000-05-31
SK282277B6 (sk) 2002-01-07
BG64348B1 (bg) 2004-11-30
NO994294D0 (no) 1999-09-03
TW508242B (en) 2002-11-01
NZ337418A (en) 2000-05-26
KR20000075897A (ko) 2000-12-26
EA199900709A1 (ru) 2000-08-28
PL190988B1 (pl) 2006-02-28
BR9807992A (pt) 2000-03-08
HK1027026A1 (en) 2001-01-05
HU224983B1 (en) 2006-05-29
EP0981334B1 (fr) 2003-05-21
PT981334E (pt) 2003-10-31
AU721851B2 (en) 2000-07-13
WO1998038983A3 (fr) 1998-12-17
CZ314899A3 (cs) 2000-03-15
NO327456B1 (no) 2009-07-06
IL131552A0 (en) 2001-01-28
ZA981832B (en) 1998-12-11
MY119722A (en) 2005-07-29
GB9704524D0 (en) 1997-04-23
DE69814850D1 (de) 2003-06-26
AP1084A (en) 2002-07-23
NO994294L (no) 1999-09-03

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